These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
195 related items for PubMed ID: 33733565
1. Collective Asymmetric Total Synthesis of C-11 Oxygenated Cephalotaxus Alkaloids. Kim JH, Jeon H, Park C, Park S, Kim S. Angew Chem Int Ed Engl; 2021 May 17; 60(21):12060-12065. PubMed ID: 33733565 [Abstract] [Full Text] [Related]
2. Novel formal synthesis of cephalotaxine via a facile Friedel-Crafts cyclization. Li WD, Wang XW. Org Lett; 2007 Mar 29; 9(7):1211-4. PubMed ID: 17348663 [Abstract] [Full Text] [Related]
3. Asymmetric total synthesis and revised structure of cephalezomine H. Taniguchi T, Yokoyama S, Ishibashi H. J Org Chem; 2009 Oct 02; 74(19):7592-4. PubMed ID: 19731926 [Abstract] [Full Text] [Related]
4. Asymmetric synthesis of the oxygenated polycyclic system of (+)-harringtonolide. Abdelkafi H, Herson P, Nay B. Org Lett; 2012 Mar 02; 14(5):1270-3. PubMed ID: 22339261 [Abstract] [Full Text] [Related]
5. Enantioselective Total Syntheses of the Cephalotaxus Alkaloids (-)-Fortuneicyclidins A and B and (-)-Cephalotine B. Sheng PZ, Ni ZB, Li LL, Wei K, Zhang H, Yang YR. Org Lett; 2023 Oct 20; 25(41):7464-7469. PubMed ID: 37800465 [Abstract] [Full Text] [Related]
8. Stereoselective synthesis of (-)-cephalotaxine and C-7 alkylated analogues. Planas L, Pérard-Viret J, Royer J. J Org Chem; 2004 Apr 30; 69(9):3087-92. PubMed ID: 15104447 [Abstract] [Full Text] [Related]
9. Asymmetric Total Syntheses of Aspidodasycarpine, Lonicerine, and the Proposed Structure of Lanciferine. Li Y, Zhu S, Li J, Li A. J Am Chem Soc; 2016 Mar 30; 138(12):3982-5. PubMed ID: 26961469 [Abstract] [Full Text] [Related]
10. Formal synthesis of cephalotaxine. Zhang ZW, Zhang XF, Feng J, Yang YH, Wang CC, Feng JC, Liu S. J Org Chem; 2013 Jan 18; 78(2):786-90. PubMed ID: 23214930 [Abstract] [Full Text] [Related]
11. Total synthesis of mersicarpine through a cationic cyclization approach. Lv Z, Li Z, Liang G. Org Lett; 2014 Mar 21; 16(6):1653-5. PubMed ID: 24555758 [Abstract] [Full Text] [Related]
12. Highly efficient formal synthesis of cephalotaxine, using the Stevens rearrangement--acid lactonization sequence as a key transformation. Sun MR, Lu HT, Wang YZ, Yang H, Liu HM. J Org Chem; 2009 Mar 06; 74(5):2213-6. PubMed ID: 19170601 [Abstract] [Full Text] [Related]
13. A formal synthesis of (-)-cephalotaxine. Esmieu WR, Worden SM, Catterick D, Wilson C, Hayes CJ. Org Lett; 2008 Jul 17; 10(14):3045-8. PubMed ID: 18549234 [Abstract] [Full Text] [Related]
15. Concise total synthesis of (±)-cephalotaxine via a transannulation strategy: development of a facile reductive oxy-Nazarov cyclization. Li WD, Duo WG, Zhuang CH. Org Lett; 2011 Jul 01; 13(13):3538-41. PubMed ID: 21650169 [Abstract] [Full Text] [Related]
16. A stereoselective asymmetric synthesis of antibiotic (-)-fumagillol using claisen rearrangement and intramolecular ester enolate alkylation as key steps. Kim D, Ahn SK, Bae H, Kim HS. Arch Pharm Res; 2005 Feb 01; 28(2):129-41. PubMed ID: 15789740 [Abstract] [Full Text] [Related]
17. A facile total synthesis of hainanensine via an unusual rearrangement--annulation cascade. Zhang ZW, Li WD. Org Lett; 2010 Apr 16; 12(8):1649-51. PubMed ID: 20235558 [Abstract] [Full Text] [Related]
18. Asymmetric synthesis of 2-alkyl-substituted tetrahydroquinolines by an enantioselective aza-Michael reaction. Taylor LL, Goldberg FW, Hii KK. Org Biomol Chem; 2012 Jun 14; 10(22):4424-32. PubMed ID: 22565504 [Abstract] [Full Text] [Related]
19. Total Synthesis and Structural Elucidation of (-)-Cephalezomine G. Jeon H, Cho H, Kim S. Org Lett; 2019 Feb 15; 21(4):1121-1124. PubMed ID: 30702299 [Abstract] [Full Text] [Related]
20. A Divergent Synthetic Route to the Vallesamidine and Schizozygine Alkaloids: Total Synthesis of (+)-Vallesamidine and (+)-14,15-Dehydrostrempeliopine. Zhang X, Anderson JC. Angew Chem Int Ed Engl; 2019 Dec 09; 58(50):18040-18045. PubMed ID: 31538685 [Abstract] [Full Text] [Related] Page: [Next] [New Search]